Canonical Allele Identifier: CA2003808897

Gene: DPAGT1

Linked Data

• dbSNP Id: rs1946422347
• gnomAD v4: 11-119097650-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097652_119097653del , CM000673.2:g.119097652_119097653del	GRCh38
NC_000011.9:g.118968362_118968363del , CM000673.1:g.118968362_118968363del	GRCh37
NC_000011.8:g.118473572_118473573del	NCBI36
NG_008918.1:g.9424_9425del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.976-101_976-100del
ENST00000524658.2:n.957-101_957-100del
ENST00000530052.2:n.1862_1863del
ENST00000682191.1:n.1322_1323del
ENST00000682192.1:n.1120-101_1120-100del
ENST00000682232.1:c.*622+203_*622+204del	ENSP00000507302.1:n.*622+203_*622+204del
ENST00000682326.1:c.917+203_917+204del	ENSP00000508129.1:n.917+203_917+204del
ENST00000682404.1:n.2019-101_2019-100del
ENST00000682517.1:n.2221_2222del
ENST00000682652.1:n.2091_2092del
ENST00000682665.1:n.1517_1518del
ENST00000682691.1:n.1517_1518del
ENST00000682791.1:c.831-101_831-100del	ENSP00000507312.1:n.831-101_831-100del
ENST00000682811.1:c.800-101_800-100del	ENSP00000508196.1:n.800-101_800-100del
ENST00000682883.1:n.1032-355_1032-354del
ENST00000682946.1:c.729-101_729-100del	ENSP00000506856.1:n.729-101_729-100del
ENST00000683143.1:c.*623-101_*623-100del	ENSP00000507168.1:n.*623-101_*623-100del
ENST00000683373.1:n.1322_1323del
ENST00000683558.1:n.1322_1323del
ENST00000683567.1:n.1027-101_1027-100del
ENST00000683955.1:n.1674-101_1674-100del
ENST00000684142.1:c.*593-101_*593-100del	ENSP00000508008.1:n.*593-101_*593-100del
ENST00000684252.1:n.1315-101_1315-100del
ENST00000684255.1:c.*623-101_*623-100del	ENSP00000507398.1:n.*623-101_*623-100del
ENST00000684315.1:n.1651-101_1651-100del
ENST00000684345.1:c.*795_*796del	ENSP00000507163.1:n.*795_*796del
ENST00000684499.1:c.*1023-101_*1023-100del	ENSP00000506800.1:n.*1023-101_*1023-100del
ENST00000684682.1:c.*548_*549del	ENSP00000507326.1:n.*548_*549del
ENST00000354202.9:c.918-101_918-100del MANE Select	ENSP00000346142.4:n.918-101_918-100del
ENST00000636404.1:c.233-589_233-588del
ENST00000638850.1:c.422-101_422-100del
ENST00000639704.1:c.825-101_825-100del	ENSP00000491336.1:n.825-101_825-100del
ENST00000640102.1:c.*571-101_*571-100del	ENSP00000492027.1:n.*571-101_*571-100del
ENST00000640747.1:c.*593-101_*593-100del	ENSP00000492730.1:n.*593-101_*593-100del
ENST00000354202.8:c.918-101_918-100del	ENSP00000346142.4:n.918-101_918-100del
ENST00000392834.7:c.*623-101_*623-100del	ENSP00000376579.3:n.*623-101_*623-100del
ENST00000409993.6:c.918-101_918-100del	ENSP00000386597.2:n.918-101_918-100del
ENST00000414373.5:c.*475-355_*475-354del	ENSP00000402019.1:n.*475-355_*475-354del
ENST00000442480.1:c.650-101_650-100del	ENSP00000406591.1:n.650-101_650-100del
ENST00000461999.1:n.984_985del
ENST00000481084.5:n.1547-101_1547-100del
ENST00000524658.1:n.223-101_223-100del
ENST00000525456.5:n.732-101_732-100del
NM_001382.3:c.918-101_918-100del	NP_001373.2:n.918-101_918-100del
XM_005271422.2:c.918-101_918-100del	XP_005271479.1:n.918-101_918-100del
XM_011542648.1:c.597-101_597-100del	XP_011540950.1:n.597-101_597-100del
XR_947801.1:n.1165-355_1165-354del
XM_005271422.3:c.918-101_918-100del	XP_005271479.1:n.918-101_918-100del
XM_011542648.2:c.597-101_597-100del	XP_011540950.1:n.597-101_597-100del
XM_017017293.2:c.597-101_597-100del	XP_016872782.1:n.597-101_597-100del
XM_017017294.2:c.729-101_729-100del	XP_016872783.1:n.729-101_729-100del
XM_017017295.1:c.402-101_402-100del	XP_016872784.1:n.402-101_402-100del
XR_001747785.2:n.952-101_952-100del
XR_947801.2:n.952-355_952-354del
NM_001382.4:c.918-101_918-100del MANE Select	NP_001373.2:n.918-101_918-100del